Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-17T19:13:27.343Z Has data issue: false hasContentIssue false

First comparison of quantitative estimates of termite biomass and abundance reveals strong intercontinental differences

Published online by Cambridge University Press:  06 February 2014

Cecilia A.L. Dahlsjö*
Affiliation:
Environmental Change Institute, School of Geography and the Environment, University of Oxford, South Parks Road, Oxford, OX1 3QY, UK Soil Biodiversity Group, Department of Entomology, The Natural History Museum, London, SW7 5BD, UK
Catherine L. Parr
Affiliation:
Department of Earth, Ocean and Ecological Sciences, School of Environmental Sciences, University of Liverpool, Liverpool, L69 3GP, UK
Yadvinder Malhi
Affiliation:
Environmental Change Institute, School of Geography and the Environment, University of Oxford, South Parks Road, Oxford, OX1 3QY, UK
Homathevi Rahman
Affiliation:
Institute for Tropical Biology and Conservation, University Malaysia Sabah, Jalan UMS, 88400 Kota Kinabalu, Sabah, Malaysia
Patrick Meir
Affiliation:
School of Geosciences, University of Edinburgh, Edinburgh, UK Research School of Biology, The Australian National University, Canberra, ACT 0200, Australia
David T. Jones
Affiliation:
Soil Biodiversity Group, Department of Entomology, The Natural History Museum, London, SW7 5BD, UK
Paul Eggleton
Affiliation:
Soil Biodiversity Group, Department of Entomology, The Natural History Museum, London, SW7 5BD, UK
*
1Corresponding author. Email: cecilia.dahlsjo@ouce.ox.ac.uk

Abstract:

Termite species and functional groups differ among regions globally (the functional-diversity anomaly). Here we investigate whether similar differences in biomass and abundance of termites occur among continents. Biomass and abundance data were collected with standardized sampling in Cameroon, Malaysia and Peru. Data from Peru were original to this study, while data from Cameroon and Malaysia were compiled from other sources. Species density data were sampled using a standardized belt transect (100 × 2 m) while the biomass and abundance measurements were sampled using a standardized protocol based on 2 × 2-m quadrats. Biomass and abundance data confirmed patterns found for species density and thus the existence of the functional diversity anomaly: highest estimates for biomass and abundance were found in Cameroon (14.5 ± 7.90 g m−2 and 1234 ± 437 ind m−2) followed by Malaysia (0.719 ± 0.193 g m−2 and 327 ± 72 ind m−2) and then Peru (0.345 ± 0.103 g m−2 and 130 ± 39 ind m−2). The biomass and abundance for each functional group were significantly different across sites for most termite functional groups. Biogeographical distribution of lineages was the primary cause for the functional diversity anomaly with true soil-feeding termites dominating in Cameroon and the absence of fungus-growing termites from Peru. These findings are important as the biomass and abundance of functional groups may be linked to ecosystem processes. Although this study allowed for comparisons between data from different regions further comparable data are needed to enhance the understanding of the role of termites in ecosystem processes on a global scale.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

LITERATURE CITED

AANEN, D. & EGGLETON, P. 2005. Fungus-growing termites originated in African rain forest. Current Biology 15:851855.Google Scholar
ARAGÃO, L. E. O. C., MALHI, Y., METCALFE, D. B., SILVA ESPEJO, J. E., JIMENEZ, E., NAVARRETE, D., ALMEIDA, S., COSTA, A. C. L., SALINAS, N., PHILLIPS, O. L., ANDERSON, L. O., ALVAREZ, E., BAKER, T. R., GONCALVEZ, P. H., HUAMAN-OVALLE, J., MAMANI-SOLORZANO, M., MEIR, P., MONTEAGUDO, A., PATINO, P., PENUELA, M. C., PRIETO, A., QUESADA, C. A., ROZAS-DAVILA, A., RUDAS, A., SILVA, J. A. & VASQUEZ, R. 2009. Above-and below-ground net primary productivity across ten Amazonian forests on contrasting soils. Biogeosciences 6:27592778.Google Scholar
BIGNELL, D. E. & EGGLETON, P. 2000. Termites in ecosystems. Pp. 363387 in Abe, T., Bignell, D. E. & Higashi, M. (eds.). Termites: evolution, sociality, symbiosis, ecology. Kluwer Academic Publishers, Dordrecht.CrossRefGoogle Scholar
BRAUMAN, A., DORÉ, J., EGGLETON, P., BIGNELL, D., BREZNAK, J. & KANE, M. 2001. Molecular phylogenetic profiling of prokaryotic communities in guts of termites with different feeding habits. FEMS Microbiology Ecology 35:2736.CrossRefGoogle ScholarPubMed
BROSSARD, M., LÓPEZ-HERNÁNDEZ, D., LEPAGE, M. & LEPRUN, J.-C. 2007. Nutrient storage in soils and nests of mound-building Trinervitermes termites in Central Burkina Faso: consequences for soil fertility. Biology and Fertility of Soils 43:437447.CrossRefGoogle Scholar
BRUSSAARD, L. 1997. Biodiversity and ecosystem functioning in soil. Ambio 26:563570.Google Scholar
BUXTON, R. 1981. Termites and the turnover of dead wood in an arid tropical environment. Oecologia 51:379384.Google Scholar
CHAPUIS-LARDY, L., BAYON, R. C., BROSSARD, M., LOPEZ-HERNANDEZ, D. & BLANCHART, E. 2011. Role of soil macrofauna in phosphorus cycling. Pp. 199214 in Brünemann, E. K., Oberson, A. & Frossard, E. (eds.). Phosphorus in action. Springer, Heidelberg.CrossRefGoogle Scholar
CONSTANTINO, R. 2002. An illustrated key to Neotropical termite genera (Insecta: Isoptera) based primarily on soildiers. Zootaxa 67:140.CrossRefGoogle Scholar
DAVIES, R., EGGLETON, P., JONES, D. T., GATHORNE-HARDY, F. J. & HERNANDEZ, L. M. 2003. Evolution of termite functional diversity: analysis and synthesis of local ecological and regional influences on local species richness. Journal of Biogeography 30:847877.CrossRefGoogle Scholar
DONOVAN, S., EGGLETON, P. & BIGNELL, D. 2001a. Gut content analysis and a new feeding group classification of termites. Ecological Entomology 26:356366.CrossRefGoogle Scholar
DONOVAN, S., EGGLETON, P. & DUBBIN, W. 2001b. The effect of a soil-feeding termite, Cubitermes fungifaber (Isoptera: Termitidae) on soil properties: termites may be an important source of soil microhabitat heterogeneity in tropical forests. Pedobiologia 11:111.CrossRefGoogle Scholar
EGGLETON, P. & TAYASU, I. 2001. Feeding groups, lifetypes and the global ecology of termites. Ecological Research 16:941960.Google Scholar
EGGLETON, P., WILLIAMS, P. & GASTON, K. 1994. Explaining global termite diversity: productivity or history? Biodiversity and Conservation 330:318330.Google Scholar
EGGLETON, P., BIGNELL, D. E., SANDS, W. A., WAITE, B., WOOD, T. G. & LAWTON, J. H. 1995. The species richness of termites (Isoptera) under differing levels of forest disturbance in the Mbalmayo forest reserve, southern Cameroon. Journal of Tropical Ecology 11:8598.Google Scholar
EGGLETON, P., BIGNELL, D. E., SANDS, W. A., MAWDSLEY, N. A., LAWTON, J. H., WOOD, T. G. & BIGNELL, N. C. 1996. The diversity, abundance and biomass of termites under differing levels of disturbance in the Mbalmayo Forest Reserve, southern Cameroon. Philosophical Transactions of the Royal Society: Biological Sciences 351:5168.Google Scholar
EGGLETON, P., HOMATHEVI, R., JONES, D. T., MACDONALD, J., JEEVA, D., BIGNELL, D. E., DAVIES, R. G. & MARYATI, M. 1999. Termite assemblages, forest disturbance and greenhouse gas fluxes in Sabah, East Malaysia. Philosophical Transactions of the Royal Society: Biological Sciences 354:17911802.CrossRefGoogle ScholarPubMed
EGGLETON, P., BIGNELL, D. & HAUSER, S. 2002. Termite diversity across an anthropogenic disturbance gradient in the humid forest zone of West Africa. Agriculture, Ecosystems and Environment 90:189202.Google Scholar
GATHORNE-HARDY, F., JONES, D. T. & MAWDSLEY, N. A. 2000. The recolonization of the Krakatau islands by termites (Isoptera), and their biogeographical origins. Biological Journal of the Linnean Society 71:251267.CrossRefGoogle Scholar
HONGOH, Y. 2010. Diversity and genomes of uncultured microbial symbionts in the termite gut. Bioscience, Biotechnology, and Biochemistry 74:11451151.CrossRefGoogle ScholarPubMed
INWARD, D., VOGLER, A. & EGGLETON, P. 2007. A comprehensive phylogenetic analysis of termites (Isoptera) illuminates key aspects of their evolutionary biology. Molecular Phylogenetics and Evolution 44:953967.CrossRefGoogle ScholarPubMed
JI, R. & BRUNE, A. 2001. Transformation and mineralization of 14 C-labeled cellulose, peptidoglycan, and protein by the soil-feeding termite Cubitermes orthognathus. Biology and Fertility of Soils 33:166174.CrossRefGoogle Scholar
JI, R. & BRUNE, A. 2005. Digestion of peptidic residues in humic substances by an alkali-stable and humic-acid-tolerant proteolytic activity in the gut of soil-feeding termites. Soil Biology and Biochemistry 37:16481655.CrossRefGoogle Scholar
JONES, C., LAWTON, J. & SHACHAK, M. 1994. Organisms as ecosystem engineers. Oikos 69:373386.Google Scholar
JONES, D. & EGGLETON, P. 2000. Sampling termite assemblages in tropical forests: testing a rapid biodiversity assessment protocol. Journal of Applied Ecology 37:191203.Google Scholar
JONES, D. T. & EGGLETON, P. 2011. Global biogeography of termites: a compilation of sources. Pp. 477498 in Bignell, D. E., Roisin, Y. & Lo, N. (eds.). Biology of termites: a modern synthesis. Springer Science+Business Media B.V., Dordrecht.Google Scholar
JOUQUET, P., DAUBER, J., LAGERLÖF, J., LAVELLE, P. & LEPAGE, M. 2006. Soil invertebrates as ecosystem engineers: intended and accidental effects on soil and feedback loops. Applied Soil Ecology 32:153164.CrossRefGoogle Scholar
JOUQUET, P., TRAORÉ, S., CHOOSAI, C., HARTMANN, C. & BIGNELL, D. 2011. Influence of termites on ecosystem functioning. Ecosystem services provided by termites. European Journal of Soil Biology 47:215222.CrossRefGoogle Scholar
LO, N. & EGGLETON, P. 2011. Termite phylogenetics and co-cladogenesis with symbionts. Pp. 2750 in Bignell, D. E., Roisin, Y. & Lo, N. (eds.). Biology of termites: a modern synthesis. Springer Science+Business Media B.V., Dordrecht.Google Scholar
NALEPA, C. A. 2011. Body size and termite evolution. Evolutionary Biology 38:243257.Google Scholar
NGUGI, D. K. & BRUNE, A. 2012. Nitrate reduction, nitrous oxide formation, and anaerobic ammonia oxidation to nitrite in the gut of soil-feeding termites (Cubitermes and Ophiotermes spp.). Environmental Microbiology 14:860871.CrossRefGoogle ScholarPubMed
NOBRE, T., EGGLETON, P. & AANEN, D. K. 2010. Vertical transmission as the key to the colonization of Madagascar by fungus-growing termites? Proceedings of the Royal Society: Biological Sciences 277:359365.Google Scholar
PALIN, O., EGGLETON, P., MALHI, Y., GIRARDIN, C., ROZAS-DAVILA, A. & PARR, C. L. 2010. Termite diversity along an Amazon–Andes elevation gradient, Peru. Biotropica 43:100107.Google Scholar
RÜCKAMP, D., AMELUNG, W., THEISZ, N., BANDEIRA, A. G. & MARTIUS, C. 2010. Phosphorus forms in Brazilian termite nests and soils: relevance of feeding guild and ecosystems. Geoderma 155:269279.Google Scholar
SCHUURMAN, G. 2005. Decomposition rates and termite assemblage composition in semiarid Africa. Ecology 86:12361249.CrossRefGoogle Scholar
VASCONCELLOS, A. & MOURA, F. 2010. Wood litter consumption by three species of Nasutitermes termites in an area of the Atlantic Coastal Forest in northeastern Brazil. Journal of Insect Science 10:19.Google Scholar
WOOD, T. G. & SANDS, W. A. 1978. The role of termites in ecosystems. Pp. 245292 in Brian, M. V. (ed.). Production ecology of ants and termites. Cambridge University Press, Cambridge.Google Scholar